Detail of "306960-77-0"

Reference

Preparation of pesticidally active aminoacetonitriles

Preparation of pesticidally active aminoacetonitriles. Steiger, Arthur; Eberle, Martin; Renold, Peter; O'Sullivan, Anthony Cornelius; Zambach, Werner (Syngenta Participations AG, Switz.). PCT Int. Appl. WO 2003004474 A1 16 Jan 2003, 58 pp. DESIGNATED STATES: W: AE, AG, AL, AM, AT, AU, AZ, BA, BB, BG, BR, BY, BZ, CA, CH, CN, CO, CR, CU, CZ, DE, DK, DM, DZ, EC, EE, ES, FI, GB, GD, GE, GH, GM, HR, HU, ID, IL, IN, IS, JP, KE, KG, KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MA, MD, MG, MK, MN, MW, MX, MZ, NO, NZ, OM, PH, PL, PT, RO, RU, SD, SE, SG, SI, SK, SL, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VN, YU, ZA, ZM, ZW, AM, AZ, BY, KG, KZ, MD, RU, TJ, TM; RW: AT, BE, BF, BJ, CF, CG, CH, CI, CM, CY, DE, DK, ES, FI, FR, GA, GB, GR, IE, IT, LU, MC, ML, MR, NE, NL, PT, SE, SN, TD, TG, TR.Some commonly used reagents like 306960-77-0 and 78-95-5 are used in this experiment. (English). (World Intellectual Property Organization).In this study，487015-47-4 is also used. CODEN: PIXXD2. CLASS: ICM: C07D239-28. ICS: C07D239-30; C07D239-34; C07D237-14; C07D241-16; C07D241-18; C07D241-24; C07D333-32; A01N043-54. APPLICATION: WO 2002-EP7515 5 Jul 2002. PRIORITY: CH 2001-1251 6 Jul 2001. DOCUMENT TYPE: Patent CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Section cross-reference(s): 5 The title compds. [I; A1, A2 = (un)substituted aryl or heteroaryl bonded via a ring carbon atom; X, Y = a bond, alkylene, alkenylene, phenylene, etc.; R1 = H, alkyl, haloalkyl; R2 = alkyl, haloalkyl, alkoxyalkyl, etc.; V = alkylene, alkenylene, alkynylene, etc.; W = O, S, SO, SO2, NR3; R3 = H, alkyl, C(O)-alkyl, alkyl-O-alkyl; n = 0-1; when n = 1, R4, R5 = H, alkyl, haloalkyl; with the provisos] and their salts, useful in controlling pests, were prepd. Thus, amidation of 2-amino-3-hydroxy-2-methylpropionitrile with 4-trifluoromethylbenzoyl chloride followed by reacting the resulting amide with 4-chloro-6-trifluoromethylpyrimidine afforded II which showed an activity of more than 80% against Aphis craccivora Diabrotica balteata, Spodoptera littoralis and Tetranychus urticae. ..