HCID 13607600, compound → HCID 21289480, compound
Reaction equation
BrC1C=CC=C2C=1CCCC2[CH2:12][CH2:13][OH:14].Cl.N1C=CC=C(CC2CCC3C=C([C:33](O)=[O:34])C=CC=3C2)C=1.[S:36]1[C:40]([CH2:41][CH2:42][CH:43]2[CH2:52][CH2:51][CH2:50][C:49]3[CH:48]=[C:47](C([O-])=O)[CH:46]=[CH:45][C:44]2=3)=[CH:39][N:38]=[CH:37]1.[Na+].Cl.[N:58]1(CCC2CCCC3C(C(O)=O)=CC=CC2=3)C=CN=C1>>[NH2:58][C:37]1[S:36][C:40]([CH2:41][CH2:42][CH:43]2[CH2:52][CH2:51][CH2:50][C:49]3[C:48]([C:33]([O:14][CH2:13][CH3:12])=[O:34])=[CH:47][CH:46]=[CH:45][C:44]2=3)=[CH:39][N:38]=1Participants
5
Procedure
5-bromo-1-(2-hydroxyethyl)-1,2,3,4-tetrahydronaphthalene was allowed to react using procedures analogous to those described in step (7) of Referential Example 1, steps (2) and (3) of Referential Example 2, steps (3), (4), (5) and (6) of Referential Example 1 and steps (5) and (6) of Referential Example 2 to give ethyl 5-(2-(2-amino-5-thiazolyl)ethyl)-5,6,7,8-tetrahydro-1-naphthalenecarboxylate as an oil.
Workup
- customto react
Sources & evidence
- ORD record
- ord-cf2a49dba59d4cd493b9a4acfa849812
- Source dataset
- uspto-grants-1988_10
- Patent number
- US04777257
Reaction notes
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