tert-Butyl 3-(hydroxymethyl)-1H-pyrrolo[2,3-b]-pyridine-1-carboxylate

Base Information

• Chemical Name: tert-Butyl 3-(hydroxymethyl)-1H-pyrrolo[2,3-b]-pyridine-1-carboxylate
• CAS No.: 144657-67-0
• Molecular Formula: C₁₃H₁₆N₂O₃
• Molecular Weight: 248.282
• Hs Code.: 2933990090
• Mol file: 144657-67-0.mol

Synonyms:tert-Butyl 3-(hydroxymethyl)-1H-pyrrolo[2,3-b]-pyridine-1-carboxylate

Chemical Property of tert-Butyl 3-(hydroxymethyl)-1H-pyrrolo[2,3-b]-pyridine-1-carboxylate

Chemical Property:

• PSA: 64.35000
• LogP: 2.31180
• Storage Temp.: 2-8°C

Purity/Quality:

97% ^*data from raw suppliers

tert-Butyl 3-(hydroxymethyl)-1H-pyrrolo[2,3-b]-pyridine-1-carboxylate >95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of tert-Butyl 3-(hydroxymethyl)-1H-pyrrolo[2,3-b]-pyridine-1-carboxylate

There total 5 articles about tert-Butyl 3-(hydroxymethyl)-1H-pyrrolo[2,3-b]-pyridine-1-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

tert-butyl 3-formyl-1H-pyrrolo[2,3-b]pyridine-1-carboxylate (144657-66-9) → tert-butyl 3-(hydroxymethyl)-1 H-pyrrolo[2,3-b]pyridine-1-carboxylate (144657-67-0)

Guidance literature:

With sodium tetrahydroborate; In methanol; at 20 ℃; for 4h;

Reference yield:

1H-pyrrolo[2,3-b]pyridin-3-carbaldehyde (4649-09-6) → tert-butyl 3-(hydroxymethyl)-1 H-pyrrolo[2,3-b]pyridine-1-carboxylate (144657-67-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) NaH / 1.) HMPA, 21 deg C, 2.) HMPA, 3 h

2: 60 percent / NaBH₄ / aq. ethanol / 4 h / 21 °C

With sodium tetrahydroborate; sodium hydride; In ethanol;

Reference yield:

di-tert-butyl dicarbonate (24424-99-5) → tert-butyl 3-(hydroxymethyl)-1 H-pyrrolo[2,3-b]pyridine-1-carboxylate (144657-67-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) NaH / 1.) HMPA, 21 deg C, 2.) HMPA, 3 h

2: 60 percent / NaBH₄ / aq. ethanol / 4 h / 21 °C

With sodium tetrahydroborate; sodium hydride; In ethanol;

upstream raw materials:

tert-butyl 3-formyl-1H-pyrrolo[2,3-b]pyridine-1-carboxylate

7-Azaindole

1H-pyrrolo[2,3-b]pyridin-3-carbaldehyde

7-azagramine

Downstream raw materials:

1-(2-methoxyl-5-chlorophenyl)-3-{1-[1-(t-butyloxycarbonyl)-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl]-1H-indol-4-yl}urea

(-)-(R)-7-azatryptophan

tert-butyl 3-(chloromethyl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate

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