2-Amino-6-methylbenzothiazole → HCID 86673641, compound

HRID 1528956Notes

Reaction equation

HRID 1528956 reaction equation
C([O:3][C:4]([C:6]1([C:9]2[CH:14]=[CH:13][C:12]([C:15]3[CH:20]=[CH:19][C:18]([C:21]4[O:25][N:24]=[C:23]([CH3:26])[C:22]=4[CH2:27]Br)=[CH:17][CH:16]=3)=[CH:11][CH:10]=2)[CH2:8][CH2:7]1)=[O:5])C.[CH3:29][C:30]1[CH:39]=[CH:38][C:33]2[N:34]=[C:35]([NH2:37])[S:36][C:32]=2[CH:31]=1>>[CH3:26][C:23]1[C:22]([CH2:27][NH:37][C:35]2[S:36][C:32]3[CH:31]=[C:30]([CH3:29])[CH:39]=[CH:38][C:33]=3[N:34]=2)=[C:21]([C:18]2[CH:17]=[CH:16][C:15]([C:12]3[CH:13]=[CH:14][C:9]([C:6]4([C:4]([OH:5])=[O:3])[CH2:8][CH2:7]4)=[CH:10][CH:11]=3)=[CH:20][CH:19]=2)[O:25][N:24]=1

Participants

3

Procedure

Prepared according to the procedure described in Example 34, Step 4, using 1-[4′-(4-bromomethyl-3-methyl-isoxazol-5-yl)-biphenyl-4-yl]-cyclopropanecarboxylic acid ethyl ester and 6-methyl-benzothiazol-2-ylamine.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-1af44ba6c94f46689ee6e48ea07a5625
Source dataset
uspto-grants-2015_07
Patent number
US09090573B2

Reaction notes

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